Genetic variations of β-MYH7 in hypertrophic cardiomyopathy and dilated cardiomyopathy

CONTEXT: Hypertrophic cardiomyopathy (HCM) is known to be manifested by mutations in 12 sarcomeric genes and dilated cardiomyopathy (DCM) is known to manifest due to cytoskeletal mutations. Studies have revealed that sarcomeric mutations can also lead to DCM. Therefore, in the present study, we have...

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Detalles Bibliográficos
Autores principales: Tanjore, Reena, RangaRaju, Advithi, Vadapalli, Shivani, Remersu, Sushant, Narsimhan, Calambur, Nallari, Pratibha
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955954/
https://www.ncbi.nlm.nih.gov/pubmed/21031054
http://dx.doi.org/10.4103/0971-6866.69348

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955954/
https://www.ncbi.nlm.nih.gov/pubmed/21031054
http://dx.doi.org/10.4103/0971-6866.69348

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